rac-1-(5-fluoro-2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)pyrimidin-4-yl)-2-hydroxypiperidine-2-carboxylic acid

ID: ALA4865417

Chembl Id: CHEMBL4865417

PubChem CID: 164622244

Max Phase: Preclinical

Molecular Formula: C23H20F2N6O4

Molecular Weight: 482.45

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(O)C1(O)CCCCN1c1nc(-c2cc(-c3ccon3)n(Cc3ccccc3F)n2)ncc1F

Standard InChI:  InChI=1S/C23H20F2N6O4/c24-15-6-2-1-5-14(15)13-31-19(17-7-10-35-29-17)11-18(28-31)20-26-12-16(25)21(27-20)30-9-4-3-8-23(30,34)22(32)33/h1-2,5-7,10-12,34H,3-4,8-9,13H2,(H,32,33)

Standard InChI Key:  XMALCNLQUALBAM-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4865417

    ---

Associated Targets(Human)

GUCY1B1 Tclin Soluble guanylate cyclase (679 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 482.45Molecular Weight (Monoisotopic): 482.1514AlogP: 3.09#Rotatable Bonds: 6
Polar Surface Area: 130.40Molecular Species: ACIDHBA: 9HBD: 2
#RO5 Violations: HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 3.18CX Basic pKa: 0.38CX LogP: 4.78CX LogD: 1.28
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.43Np Likeness Score: -1.15

References

1. Rennie GR, Barden TC, Bernier SG, Carvalho A, Deming R, Germano P, Hudson C, Im GJ, Iyengar RR, Jia L, Jung J, Kim E, Lee TW, Mermerian A, Moore J, Nakai T, Perl NR, Tobin J, Zimmer DP, Renhowe PA..  (2021)  Discovery of CYR715: A novel carboxylic acid-containing soluble guanylate cyclase stimulator.,  40  [PMID:33662540] [10.1016/j.bmcl.2021.127886]

Source